Additional file 4: of Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery
收藏数据链接：
官方服务：
资源简介：
Enrichment of non-synonymous DNM from patients with neurodevelopmental disease. (XLSX 107 kb)
神经发育疾病患者非同义新发突变（de novo mutation, DNM）富集数据集（XLSX格式，大小107 KB）
创建时间：
2016-12-14
